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Research 121–150 of 140
- Primary cicatricial alopecias
- Impacto del desequilibrio del microbioma del cuero cabelludo en la severidad de la alopecia areata, marcadores inflamatorios y cambios post-tratamiento
- Hair Transplantation in Migraine Headache Patients
- Cochlea hair cell rescue after a noise-induced hearing loss using a low level laser therapy (LLLT)
- Adult bone-marrow-derived mesenchymal stem cells contribute to wound healing of skin appendages
- Hair That Is Difficult to Manage in a Hispanic Girl
- SkIndia Quiz 24: Itchy papules over face
- Two Clinically Unusual Cases of Folliculotropic Mycosis Fungoides: One with and the Other without Syringotropism
- Overnight loss of pigmented hair in autoimmune autonomic neuropathy treated with IVIg
- Culture Strategy Determines the Differentiation Status of Sweat Gland Cells
- Identification of Stem Cell Populations in Sweat Glands and Ducts Reveals Roles in Homeostasis and Wound Repair
- Risk Factors and Characterization of Vitiligo and Alopecia Areata in Patients With Chronic Graft-vs-Host Disease
- Utilities of Botulinum Toxins in Dermatology and Cosmetology
- Eruptive vellus hair cysts: An underdiagnosed entity
- The Non-Cosmetic Dermatological Use of Botulinum Neurotoxin
- Cutaneous Neuroimmune Interactions in Peripheral Neuropathic Pain States
- The skin landscape in diabetes mellitus. Focus on dermocosmetic management
- Cephalalgic Alopecia Areata
- Cutaneous manifestations of endocrine diseases in children
- Systemic cyproterone acetate and 5% minoxidil topical in the treatment of female pattern hair loss
- Genotype-phenotype correlation in boys with X-linked hypohidrotic ectodermal dysplasia
- Congenital insensitivity to pain with anhidrosis and progressing acro-osteolysis: a case report with 7-year follow-up
- Scleromyxedema with neurologic involvement: Therapy with intravenous immunoglobulin
- Store-operated calcium channels in skin
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Molecular basis of hypohidrotic ectodermal dysplasia: an update